Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of WS AudiologyLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Rexton with 21 510(k) clearances. The most recent is a 510(k) clearance dated Mar 28, 1997: REXTON MODEL 48 AND 49PP.
| Mar 28, 1997 | REXTON MODEL 48 AND 49PPK970537 · ESD | 510(k) clearances |
| Nov 27, 1996 | PICCOLO K-AMP VC+, PICCOLO P-A1, PICCOLO P-AO AND PICCOLO ATCK964451 · ESD | 510(k) clearances |
| Mar 22, 1996 | LONG LIFE RX-12K960295 · ESD | 510(k) clearances |
| Jan 17, 1996 | REXTON'S HORIZION FAMILY OF MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMBALE INSTRUMENTSK954922 · ESD | 510(k) clearances |
| Sep 18, 1995 | REXTON MINI-PRIMO PLUS, PP142, D.C .H.I. FAMILYK953770 · ESD | 510(k) clearances |
| Mar 21, 1995 | M-29 PP-PC, M-29 PP-O/PCK950451 · ESD | 510(k) clearances |
| Feb 22, 1995 | MICRO MINI PRIMO AGC, MICRO-MINI PRIMO S-AGCK944851 · ESD | 510(k) clearances |
| Dec 30, 1994 | ORION PPM, PP, PP-DK944777 · ESD | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
